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Symbol
Name
ID
Kit
KIT proto-oncogene receptor tyrosine kinase
MGI:96677
Phenotype annotations related to hearing/vestibular/ear
*Aspects of the system are reported to show a normal phenotype.
Darker colors indicate more annotations
Human Phenotypes
Abnormality of the ear
Hearing impairment
Disease(s) Associated with KIT
piebaldism

Mouse Phenotypes
hearing/vestibular/ear phenotype
abnormal stria vascularis vasculature morphology
abnormal ear pigmentation
decreased ear pigmentation
abnormal cochlea morphology
abnormal cochlear outer hair cell morphology
cochlear hair cell degeneration
abnormal organ of Corti morphology
organ of Corti degeneration
abnormal stria vascularis morphology
abnormal strial basal cell morphology
absent strial intermediate cells
abnormal strial marginal cell morphology
thin stria vascularis
abnormal tectorial membrane morphology
vestibular hair cell degeneration
abnormal vestibular saccule morphology
abnormal otolith morphology
enlarged otoliths
absent endocochlear potential
increased or absent threshold for auditory brainstem response
deafness
Availability Mouse Genotype
KitW-v/KitW-v
KitWads/KitWads
KitW-2Btlr/Kit+
KitW-85J/Kit+ *

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
04/16/2024
MGI 6.23
The Jackson Laboratory